A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520629



Internal ID18472224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13014538..13028949hg38UCSC Ensembl
Innerchr10:13056538..13070949hg19UCSC Ensembl
Innerchr10:13096544..13110955hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3814412
hg1914412
hg1814412
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051704
Supporting Variants
Samples
Known GenesCCDC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3520629
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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